Please correct answer and don't use hand rating If the other boronate ester is used to synthesize the biaryl compound, what would be the appropriate bromo compound.Draw a molecule on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars, including charges whereneeded.יH EXP CONT ?HCN

The question asks to draw the appropriate bromo compound for the synthesis of a biaryl compound…

Answered: If the other boronate ester is used to…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter9: Alkynes: An Introduction To Organic Synthesis

Section9.SE: Something Extra

Problem 56AP

See similar textbooks

Similar questions

I'm stuck on step 3. Please help, thank you
Treatment of acetylene with a suitable base affords lithium acetylide, which was used as a reagent in a partial synthesis of the antitumor natural product (+)-acutiphycin. (Org. Lett. 2014, 16, 1168-1171) Possible bases to consider H-C=C-H Acetylene Step 1 Li :Base T H-O: Li Lithium hydroxide (LiOH) three steps Lithium acetylide Draw the structure of lithium acetylide. Draw Your Solution di. Η Η Η Η | | | | H-C-C-C-C: II HH HH Butyllithium (BuLi) OR CEC- Li OH CH3 -H CH3 Lithium diisopropyl amide (LDA) OMe H3C H H₂C many steps Li HO OH I (+)-Acutiphycin CH3 CH₂ "OH
The question is: "Draw the curved arrow mechanism for the reaction between pentan-2-one and (CH3)3O– in t-butanol to form an enolate. Draw all electrons and charges on both resonance structures. Then answer the question about the reaction." I got the initial arrows correct, but am not entirely sure what the carbanion intermediate would look like and then what the curved arrows would be to convert it to its final oxanion form
Need help solving this, please show your work with the answer!
Complete the mechanism for the hydrolysis below by adding any missing bonds, charges, nonbonding electrons, and curved arrows.
20:33 1 : ●●● all the proper notations for depicting resonance. 4. Provide the full mechanism (curved arrows and intermediates) that leads to the product in the scheme below. Draw the structure of the product to help you see how the starting materials will combine. Use that as a clue to figure out how to draw the mechanism arrows. ccare in your scheme. Be sure to use NaOEt 00 i 5. Provide the major organic product of the reaction shown. Determine if these conditions are best for SN2, SN1, E2, or E1. Be sure to indicate stereochemistry by using the proper wedges/dashes in the product. acetone phenyl butanoate Send a chat O
Below is a structure of Levonorgestrel (Plan B®), used in prevention of pregancy. но HH H. Levonorgestrel Plan B® Below is one of the reactions used in the synthesis. What type of reaction is it? он :CEC-H Lc=c-H THF as solvent Levonorgestrel H,CO H,CO O A grignard reaction. Nucleophilic acyl substitution. O Nucleophilic addition. O An SN2 reaction. O O
Don't use hand raiting please
Can you please help me with these ester hydrolysis questions?
The blcyclic ketone shown below is first treaterd with a base, then ethyliodide is added to form the substituted ketone. Which base/conditions are sultable? 1) Base 2) O 1. Lithium diisopropylamide in THF at -78 "C. O 2. NaBH4 in methanol at room temperature. O 3. Sodium methoxide in methanol at room temperature. O 4. DBU in THF at 25 "C.
10:54 ← Question 21 of 32 Draw the major product of this reaction. Ignore inorganic byproducts. Submit Assume that the water side product is continuously removed to drive the reaction toward products. (CH3)2NH, TSOH Select to Draw | I I
3. Draw compounds A-G in the space below the scheme using line notation ΟΞ A: hexanoic acid B: 1-heptyne SOCI₂ HgSO4, H2SO4 H₂O E C (CH3)2CuLi MgBr F NaOCl, HOAc D 1. CH3CHO 2. H₂Ot G HCN 1. 03 2. Me₂S (acetone is a by product of the reaction from E to D) 1. PhMgBr 2. H₂O H

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS

If the other boronate ester is used to synthesize the biaryl compound, what would be the appropriate bromo compound. Draw a molecule on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars, including charges where needed. י H EXP CONT ? H C N